Endo-Kerrison Shaft EKS15554090

GUDID 04250337120261

Endo-Kerrison Shaft

Joimax GmbH

Rigid endoscopic biopsy forceps, reusable
Primary Device ID04250337120261
NIH Device Record Key4e58fa60-e109-4cce-96e4-99ec32819447
Commercial Distribution StatusIn Commercial Distribution
Brand NameEndo-Kerrison Shaft
Version Model NumberEKS15554090
Catalog NumberEKS15554090
Company DUNS344267187
Company NameJoimax GmbH
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337120261 [Primary]

FDA Product Code

LRYPunch, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


[04250337120261]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-09
Device Publish Date2023-09-29

On-Brand Devices [Endo-Kerrison Shaft]

04250337120285Endo-Kerrison Shaft
04250337120278Endo-Kerrison Shaft
04250337120261Endo-Kerrison Shaft
04250337120254Endo-Kerrison Shaft
04250337120247Endo-Kerrison Shaft

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